Product Recalls in Alaska
Product recalls affecting Alaska — including food, drugs, consumer products, medical devices, and vehicles distributed to Alaska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,311 recalls have been distributed to Alaska in the last 12 months.
Showing 37161–37180 of 46,762 recalls
Recalled Item: Garden Lites Kale & Quinoa Souffle Recalled by classic cooking llc Due to...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: classic cooking Kale and Quinoa Cake Recalled by classic cooking llc Due to...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Garden Lites Veggie Bites Kale & Brown Rice Recalled by classic cooking llc...
The Issue: Cumin contains undeclared peanut protein
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: HT Traders Blue Cheese Jalapeno Spicy & Unique Seasoning Blend Recalled by...
The Issue: The products contain cumin that may be contaminated with undeclared peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dark Chili Powder packaged in the following configurations: (1) a Recalled...
The Issue: The products contain cumin that may be contaminated with undeclared peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Archer Farms Cumin Recalled by Brinkhoff & Monoson Inc Due to Undeclared Peanut
The Issue: The products contain cumin that may be contaminated with undeclared peanut...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ARCHITECT c4000 Cuvette Segment Recalled by Abbott Laboratories, Inc Due to...
The Issue: There is a potential to generate falsely-depressed patient results in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Trifurcated set with Bionectors and check valves Recalled by Churchill...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore T-Port Set Recalled by Churchill Medical Systems, Inc. Due to...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore Trifurcated Ext set Recalled by Churchill Medical Systems, Inc....
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" Trifurcated set with Bionectors Recalled by Churchill Medical Systems,...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Standard Bore High Pressure Ext Set Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4" Microbore Double Lumen Set with Bionector Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6" Trifurcated Extension Set Recalled by Churchill Medical Systems, Inc. Due...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" High Pressure Set with Bionector Recalled by Churchill Medical Systems,...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 8" Standard Bore Ext Set Recalled by Churchill Medical Systems, Inc. Due to...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bifurcated set with check vales and Bionectors Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7" Standard Bore High Pressure Ext Set Recalled by Churchill Medical...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bifircated Extension Set Recalled by Churchill Medical Systems, Inc. Due to...
The Issue: Potential for leaking caused by insufficient bond between needleless device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TDX Electric Wheelchair. Invacare FDX Recalled by Invacare Corporation Due...
The Issue: If the slack in the wires is not routed and secured correctly, flexing of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.